Localization of Multiple Melanoma Tumor–Suppressor Genes on Chromosome 11 by Use of Homozygosity Mapping-of-Deletions Analysis
- 1 August 2000
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 67 (2), 417-431
- https://doi.org/10.1086/302999
Abstract
No abstract availableKeywords
This publication has 91 references indexed in Scilit:
- Genomic organization and precise physical location of protein phosphatase 2A regulatory subunit A beta isoform gene on chromosome band 11q23Gene, 1998
- A High-Resolution STS, EST, and Gene-Based Physical Map of the Hereditary Paraganglioma Region on Chromosome 11q23Genomics, 1997
- A 1-Mb Physical Map and PAC Contig of the Imprinted Domain in 11p15.5 That Contains TAPA1 and the BWSCR1/WT2 RegionGenomics, 1997
- Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancersNature Genetics, 1997
- Allele loss on chromosome 11q and microsatellite instability in malignant melanomaEuropean Journal Of Cancer, 1996
- A Yeast Artificial Chromosome Contig andNotI Restriction Map That Spans the Tumor Suppressor Gene(s) Locus, 11q22.2–q23.3Genomics, 1996
- Metastasis suppressed, but tumorigenicity and local invasiveness unaffected, in the human melanoma cell line MelJuSo after introduction of human chromosomes 1 or 6Molecular Carcinogenesis, 1996
- On the oncodevelopmental role of human imprinted genesMedical Hypotheses, 1994
- Preferential chromosome 11q and/or 17q aberrations in short-term cultures of metastatic melanoma in resections from human brainCancer Genetics and Cytogenetics, 1992
- Relation of Cytogenetic Abnormalities and Clinical Outcome in Metastatic MelanomaNew England Journal of Medicine, 1990